Other mutations in this stock |
Total: 62 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aasdh |
A |
T |
5: 77,044,445 (GRCm39) |
D148E |
probably benign |
Het |
Abca13 |
A |
G |
11: 9,531,665 (GRCm39) |
I4631V |
probably damaging |
Het |
Adamts16 |
A |
T |
13: 70,886,617 (GRCm39) |
W1058R |
probably damaging |
Het |
Adgrf5 |
A |
G |
17: 43,741,586 (GRCm39) |
I163V |
probably null |
Het |
Ano1 |
T |
A |
7: 144,201,774 (GRCm39) |
Y338F |
probably damaging |
Het |
Atp4a |
A |
G |
7: 30,418,521 (GRCm39) |
D603G |
probably damaging |
Het |
Bmp2k |
GGCCCGC |
GGC |
5: 97,235,050 (GRCm39) |
|
probably null |
Het |
Brinp2 |
T |
C |
1: 158,074,156 (GRCm39) |
D655G |
probably benign |
Het |
C3ar1 |
A |
G |
6: 122,827,321 (GRCm39) |
S299P |
probably benign |
Het |
Calhm1 |
T |
A |
19: 47,132,058 (GRCm39) |
|
probably null |
Het |
Ccdc187 |
G |
A |
2: 26,166,104 (GRCm39) |
P775L |
possibly damaging |
Het |
Cd27 |
A |
G |
6: 125,213,561 (GRCm39) |
F48S |
probably damaging |
Het |
Cfap52 |
A |
G |
11: 67,844,947 (GRCm39) |
Y41H |
possibly damaging |
Het |
Cntn5 |
A |
G |
9: 9,748,394 (GRCm39) |
S701P |
possibly damaging |
Het |
Ctbp2 |
G |
T |
7: 132,597,088 (GRCm39) |
A665D |
probably damaging |
Het |
Ctsd |
C |
A |
7: 141,937,266 (GRCm39) |
G81C |
probably damaging |
Het |
Cybb |
C |
G |
X: 9,316,989 (GRCm39) |
D246H |
probably benign |
Het |
Dpysl4 |
C |
T |
7: 138,671,853 (GRCm39) |
A67V |
probably benign |
Het |
Dst |
C |
T |
1: 34,218,438 (GRCm39) |
T1626I |
probably damaging |
Het |
Etfdh |
A |
C |
3: 79,523,261 (GRCm39) |
D217E |
probably null |
Het |
Far1 |
T |
A |
7: 113,167,396 (GRCm39) |
Y494N |
probably damaging |
Het |
Fndc1 |
G |
A |
17: 7,990,366 (GRCm39) |
T1110M |
unknown |
Het |
Frmd4a |
G |
T |
2: 4,488,876 (GRCm39) |
D78Y |
probably damaging |
Het |
Fsip2 |
G |
A |
2: 82,808,260 (GRCm39) |
M1526I |
probably benign |
Het |
Ggn |
C |
T |
7: 28,871,777 (GRCm39) |
P399S |
probably damaging |
Het |
H2ac6 |
C |
T |
13: 23,867,888 (GRCm39) |
G5S |
probably damaging |
Het |
Hap1 |
A |
G |
11: 100,246,600 (GRCm39) |
W102R |
probably damaging |
Het |
Herc2 |
T |
A |
7: 55,846,938 (GRCm39) |
S3629R |
possibly damaging |
Het |
Hyal4 |
A |
C |
6: 24,765,861 (GRCm39) |
Y405S |
possibly damaging |
Het |
Ifi204 |
G |
A |
1: 173,580,325 (GRCm39) |
T395I |
probably damaging |
Het |
Igsf9 |
A |
G |
1: 172,326,005 (GRCm39) |
E1147G |
probably damaging |
Het |
Inpp5a |
T |
A |
7: 139,118,097 (GRCm39) |
I225N |
possibly damaging |
Het |
Kcnv1 |
T |
C |
15: 44,972,518 (GRCm39) |
K455R |
probably damaging |
Het |
Kmt2c |
T |
C |
5: 25,515,455 (GRCm39) |
D2796G |
probably benign |
Het |
Ngp |
A |
T |
9: 110,251,401 (GRCm39) |
D143V |
probably benign |
Het |
Nlrp5 |
T |
C |
7: 23,118,264 (GRCm39) |
C663R |
possibly damaging |
Het |
Nup205 |
G |
T |
6: 35,204,615 (GRCm39) |
R1469L |
probably damaging |
Het |
Nup205 |
T |
A |
6: 35,207,483 (GRCm39) |
F1512I |
probably damaging |
Het |
Nwd1 |
T |
C |
8: 73,397,542 (GRCm39) |
S594P |
probably damaging |
Het |
Nxpe2 |
A |
C |
9: 48,230,875 (GRCm39) |
V498G |
probably benign |
Het |
P3h4 |
G |
A |
11: 100,302,677 (GRCm39) |
R320C |
probably damaging |
Het |
Plec |
A |
G |
15: 76,063,455 (GRCm39) |
L2273P |
probably damaging |
Het |
Ppp1r14b |
C |
T |
19: 6,953,951 (GRCm39) |
L100F |
probably damaging |
Het |
Ralgps2 |
C |
T |
1: 156,660,234 (GRCm39) |
|
probably null |
Het |
Rrp12 |
C |
T |
19: 41,868,591 (GRCm39) |
G584D |
possibly damaging |
Het |
Scamp3 |
T |
C |
3: 89,088,504 (GRCm39) |
F237L |
probably damaging |
Het |
Scn10a |
A |
G |
9: 119,464,507 (GRCm39) |
|
probably null |
Het |
Sh3bp5 |
C |
A |
14: 31,099,452 (GRCm39) |
R265L |
probably benign |
Het |
Shroom1 |
A |
T |
11: 53,354,818 (GRCm39) |
D246V |
probably benign |
Het |
Snapc4 |
T |
A |
2: 26,268,618 (GRCm39) |
E14D |
probably damaging |
Het |
Spag5 |
A |
T |
11: 78,194,972 (GRCm39) |
Q93L |
probably benign |
Het |
Tcstv5 |
T |
A |
13: 120,411,501 (GRCm39) |
Q35L |
probably benign |
Het |
Tle1 |
C |
T |
4: 72,038,372 (GRCm39) |
|
probably null |
Het |
Ttll10 |
G |
A |
4: 156,119,438 (GRCm39) |
P683S |
possibly damaging |
Het |
Unc13c |
A |
C |
9: 73,719,649 (GRCm39) |
D1006E |
probably benign |
Het |
Unc80 |
A |
T |
1: 66,732,955 (GRCm39) |
K3101N |
possibly damaging |
Het |
Vdac1 |
A |
G |
11: 52,278,280 (GRCm39) |
Y247C |
possibly damaging |
Het |
Vmn2r1 |
G |
A |
3: 63,997,474 (GRCm39) |
V377I |
probably benign |
Het |
Vmn2r23 |
A |
G |
6: 123,710,352 (GRCm39) |
T552A |
probably damaging |
Het |
Xrcc3 |
C |
T |
12: 111,771,044 (GRCm39) |
R295Q |
probably damaging |
Het |
Zfp780b |
T |
C |
7: 27,664,243 (GRCm39) |
N104S |
probably benign |
Het |
Zkscan17 |
A |
G |
11: 59,378,397 (GRCm39) |
V262A |
possibly damaging |
Het |
|
Other mutations in Prlhr |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00094:Prlhr
|
APN |
19 |
60,456,119 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02306:Prlhr
|
APN |
19 |
60,456,353 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02398:Prlhr
|
APN |
19 |
60,455,753 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02506:Prlhr
|
APN |
19 |
60,456,366 (GRCm39) |
missense |
probably damaging |
1.00 |
R0718:Prlhr
|
UTSW |
19 |
60,456,497 (GRCm39) |
nonsense |
probably null |
|
R0718:Prlhr
|
UTSW |
19 |
60,456,443 (GRCm39) |
missense |
probably benign |
0.00 |
R1829:Prlhr
|
UTSW |
19 |
60,455,867 (GRCm39) |
missense |
probably damaging |
1.00 |
R1886:Prlhr
|
UTSW |
19 |
60,455,932 (GRCm39) |
nonsense |
probably null |
|
R4493:Prlhr
|
UTSW |
19 |
60,455,519 (GRCm39) |
missense |
probably benign |
0.04 |
R4494:Prlhr
|
UTSW |
19 |
60,455,519 (GRCm39) |
missense |
probably benign |
0.04 |
R4495:Prlhr
|
UTSW |
19 |
60,455,519 (GRCm39) |
missense |
probably benign |
0.04 |
R5869:Prlhr
|
UTSW |
19 |
60,456,059 (GRCm39) |
missense |
probably damaging |
0.96 |
R5886:Prlhr
|
UTSW |
19 |
60,456,014 (GRCm39) |
nonsense |
probably null |
|
R7651:Prlhr
|
UTSW |
19 |
60,455,583 (GRCm39) |
missense |
probably benign |
0.13 |
R7809:Prlhr
|
UTSW |
19 |
60,456,293 (GRCm39) |
missense |
probably damaging |
1.00 |
R8141:Prlhr
|
UTSW |
19 |
60,455,747 (GRCm39) |
missense |
probably damaging |
1.00 |
R8337:Prlhr
|
UTSW |
19 |
60,456,284 (GRCm39) |
missense |
possibly damaging |
0.88 |
R8481:Prlhr
|
UTSW |
19 |
60,456,125 (GRCm39) |
missense |
possibly damaging |
0.95 |
R8560:Prlhr
|
UTSW |
19 |
60,456,635 (GRCm39) |
start gained |
probably benign |
|
Z1177:Prlhr
|
UTSW |
19 |
60,455,753 (GRCm39) |
missense |
probably damaging |
1.00 |
|